The Centre for Business Intelligence’s 4th Clinical Supply Chain Management Conference taking place at the Hyatt Regency Princeton New Jersey today and tomorrow (30th and 31st July) will provide a forum for discussion on a variety of topics including labelling regulatory compliance, shipping requirements, and how to increase efficiency of labelling operations.
Bob Brunk, PrisymID’s West Coast US Sales Manager is traveling to New Jersey to deliver a presentation focusing on the use of a dedicated Label Management Systems such as Prisym Medica and Prisym Medica ClinTrial. Bob will describe how using a dedicated designed for purpose solution can improve the efficiency of any organization looking to package and label clinical trial supplies and comply with regulations such as FDA 21 CFR Part 11.
Prisym Medica and Prisym Medica ClinTrial enables many of the worlds largest Clinical Trials outsourcing companies to operate efficiently, and has helped many smaller organizations become more efficient and effective.
Bob will describe some of the advantages that Prisym Medica ClinTrial offers our customers.
- ACCURATE – Through automated version control and approval management
- PRECISE – Label design is easy to create & approve
- COLLABORATIVE – Labels and trial data are centralized and can be access wherever you need it
- FLEXIBLE – Trial data can be randomized or imported
- EFFICIENT – Labels can be generated at the touch of a button
- COMPLIANT – Gives organizations the tools to become 21 CFR Part 11
I really like your blog and i respect your work. I’ll be a frequent visitor.
Interesting and informative. But will you write about this one more?
Very interesting and amusing subject. I read with great pleasure.
I added your blog to bookmarks. And i’ll read your articles more often!